Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Sema3b ENSRNOG00000016512

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Description

semaphorin 3B [Source:RGD Symbol;Acc:1310079]

Gene Synonyms

LOC363142

Location

Primary_assembly 8: 117,150,589-117,157,658 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 1 transcript (splice variant), 205 orthologues, 19 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000066296.3	Sema3b-201	2511	749aa	ENSRNOP00000060214.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZHJ3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Paralogues

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